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NCT07637500
Clinical Trial
Refocus VisAbility™ Micro Insert System Pre-market Clinical Trial
Recruiting
View on ClinicalTrials.gov →
Summary
The primary study objective is to evaluate the safety and effectiveness of the VisAbility™ Micro Insert System for improvement in binocular distance corrected near visual acuity in presbyopic patients.
Trial Details
NCT Number
NCT07637500
Lead Sponsor
Refocus Group, Inc.
Conditions
Presbyopia
Enrollment
33 participants
Start Date
2026-06-02
Primary Completion
2027-12
(estimated)
Study Completion
2027-12
(estimated)
Updated on ClinicalTrials.gov
2026-06-09